Light Bioscience, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Light Bioscience, LLC makes
Light Bioscience, LLC manufactures LED photomodulation devices, including consumer and professional-grade models designed for localized light therapy. These devices emit specific wavelengths to target skin and tissue conditions, such as inflammation or wound healing, through non-invasive photomodulation technology.
The company’s portfolio is regulated under FDA’s Class II device classification, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry, and the manufacturer operates from the United States.
Catalogue
Gentlewaves Consumer Led Photomodulation Device Ref K062991
Regimes: 510(k) Registry: 510(k)Gentlewaves Led Photomodulation Device Ref K031425
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Light Bioscience, LLC have in the registry?
The registry currently lists 2 devices for Light Bioscience, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Light Bioscience, LLC's devices?
Among its 2 most recently registered devices, Light Bioscience, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Light Bioscience, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Light Bioscience, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Light Bioscience, LLC in the registry?
The most recently registered devices listed for Light Bioscience, LLC include GENTLEWAVES CONSUMER LED PHOTOMODULATION DEVICE and GENTLEWAVES LED PHOTOMODULATION DEVICE.